The USA Bans 26 Drugs Including 2C* Family, Mephedrone, MDPV and Synthetic Cannabinoids
Update: Post mortem has confirmed that the Miami cannibal was not high on bath salts, LSD or synthetic cannabinoids.
The USA yesterday booted a host of previously unregulated drugs in to the “schedule 1″ bracket. The move appears to be a knee-jerk reaction to recent events such as the “bath salt zombie attack”, believed by the police (apparently based upon nothing but pure guesswork) to be related to “bath salts”, the name euphemistically given to unscheduled drugs when it is not clear from the packaging what chemical(s) a drug contains. If you think that sounded confused, you’d be right – in classic McCarthyist style, a whole host of drugs have been banned despite there having been no research in to their effects whatsoever.
The newly classified schedule 1 drugs are as follows, effective October 1st 2012:
‘(i) 5-(1,1-dimethylheptyl)-2-[(1R,3S)-3-hydroxycyclohexyl]-phenol (CP-47,497);
‘(ii) 5-(1,1-dimethyloctyl)-2-[(1R,3S)-3-hydroxycyclohexyl]-phenol (cannabicyclohexanol or CP-47,497 C8-homolog);
1-pentyl-3-(1-naphthoyl)indole (JWH-018 and AM678);
1-butyl-3-(1-naphthoyl)indole (JWH-073);
1-hexyl-3-(1-naphthoyl)indole (JWH-019);
1-[2-(4-morpholinyl)ethyl]-3-(1-naphthoyl)indole (JWH-200);
1-pentyl-3-(2-methoxyphenylacetyl)indole (JWH-250);
1-pentyl-3-[1-(4-methoxynaphthoyl)]indole (JWH-081);
1-pentyl-3-(4-methyl-1-naphthoyl)indole (JWH-122);
1-pentyl-3-(4-chloro-1-naphthoyl)indole (JWH-398);
1-(5-fluoropentyl)-3-(1-naphthoyl)indole (AM2201);
1-(5-fluoropentyl)-3-(2-iodobenzoyl)indole (AM694);
1-pentyl-3-[(4-methoxy)-benzoyl]indole (SR-19 and RCS-4);
1-cyclohexylethyl-3-(2-methoxyphenylacetyl)indole (SR-18 and RCS-8); and
1-pentyl-3-(2-chlorophenylacetyl)indole (JWH-203).’.
4-methylmethcathinone (Mephedrone).
3,4-methylenedioxypyrovalerone (MDPV).
2-(2,5-Dimethoxy-4-ethylphenyl)ethanamine (2C-E).
2-(2,5-Dimethoxy-4-methylphenyl)ethanamine (2C-D).
2-(4-Chloro-2,5-dimethoxyphenyl)ethanamine (2C-C).
2-(4-Iodo-2,5-dimethoxyphenyl)ethanamine (2C-I).
2-[4-(Ethylthio)-2,5-dimethoxyphenyl]ethanamine (2C-T-2).
2-[4-(Isopropylthio)-2,5-dimethoxyphenyl]ethanamine (2C-T-4).
2-(2,5-Dimethoxyphenyl)ethanamine (2C-H).
2-(2,5-Dimethoxy-4-nitro-phenyl)ethanamine (2C-N).
2-(2,5-Dimethoxy-4-(n)-propylphenyl)ethanamine (2C-P).’.
It’s not surprising to see MDPV on the list, as MDPV is a primary culprit in many drugs marketed in the US as “bath salts”. MDPV, often likened to PCP, is a drug known for a range of thoroughly unpleasant side-effects. Some of the other drugs on the list are somewhat more surprising however. It is particularly bizarre to see the 2C* family described as “new” drugs by the US DEA, the 2C* family was of course first synthesised by Alexander Shulgin over three decades ago and has been known for its unusual blend of psychedelic and aphrodisiac qualities ever since. Like many psychedelics, the 2c* family is also known for its relatively low-risk toxicity profile (it is highly active at doses on the miligram range while relatively high doses have been reported with few ill effects). The US DEA have cited only one instance of overdose through improper use of 2c-E as justification for the ban of the entire 2c* family.
Paradoxically, the newly listed Schedule 1 drugs are to be defined as having:
“A high potential for abuse.. no medical use in treatment in the United States; and lack an accepted safety for use of the drug”
This is an ironic definition considering that not only is there a complete lack of human research for most of the drugs listed above, but now that these drugs are scheduled it is near impossible for US scientists, like UK scientists before them, to study these drugs to determine whether there could ever be a medical use for any of the drugs. It doesn’t take a genius to see how this vicious cycle could end badly. We will likely witness the chemicals above rapidly dumped on the underground market, to risk being mislabelled and sold as cutting agents. There is now little incentive for pharmaceutical companies to investigate relations of the drugs as they are now likely controlled under analogue legislation. Furthermore, there is now every incentive for underground drugs manufacturers to develop new drugs, with new unknown risks and contraindications, to be unleashed on the next generation of guinea pigs – and the self-defeating logic of the drug war once again prevails.
If you liked this, you may also like:
-
Anonymous
-
Brad
-
AJ
Recent Posts
The future of a home computer controlled by your eyes may be far closer than you think
The Neuroscience Power Crisis: What’s the fallout?
Now you can enlarge and denoise your photos, all thanks to basic research
Achieving herd immunity against pseudoscience in the age of the filter bubble and the social news revolution
The Moving Goalposts of Mental Illness
Don’t Drink The Kool-Aid
In Defence of Pseudonyms in Science: Defending the Right to Write
How will the UK ban on doctors using social media anonymously affect patients?
The bad science of Satoshi Kanazawa
Academic Copyright: The bad news and the good news
Subscribe
Enter your email address to subscribe. You can make contact directly by simply hitting reply to the email. You will never receive spam under any circumstances and you can unsubscribe at any time with one click. Alternately, use the link below to subscribe via RSS or your favourite reading platform.
Twitter
Facebook
Hash Cloud
Africa America Bad Science BCI Brain Computer Interfacing breaking news Cannabis Censorship Cocaine Copyright Counterfeit Drugs Daily Fail DailyFail daily mail Daily Mail Demolition Squad Drugs EEG Emotiv Fake Drugs FMRI Health Hoax Independent Misinformation Music Neuroscience Open Science Procrastination Psychology Rat Brain Robot Review Satire Science sex Skepticism Statistics Student Loans Crisis Susan Greenfield Synaesthesia Technology The confederacy of dunces Video walking War on Drugs Wikileaks
WP Cumulus Flash tag cloud by Roy Tanck requires Flash Player 9 or better.















